QC Analyst

JR United Kingdom; Preston; On-site; GBP 30,000 - 35,000; Full time

Job summary

A well-established GMP-accredited pharmaceutical manufacturer in Lancashire is seeking a skilled QC Analyst. The role involves ensuring the safety and compliance of pharmaceutical products through rigorous analytical testing. The ideal candidate will have a relevant degree and experience in a GMP-regulated environment, with opportunities for professional development and career progression.

Benefits

Professional Development

Ongoing Training

Career Progression

Qualifications

• 1-3 years of experience in a GMP-regulated pharmaceutical laboratory.
• Proficient in HPLC; experience with GC, UV, and IR is advantageous.

Responsibilities

• Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.
• Operate and maintain analytical instruments including HPLC, GC, UV, and IR.
• Ensure strict adherence to cGMP and internal quality standards.

Skills

Attention to Detail

Analytical Techniques

Education

BSc in Chemistry

BSc in Pharmaceutical Sciences

Tools

HPLC

GC

UV

IR

Job description

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Our client is a well-established, GMP-accredited pharmaceutical manufacturer based in Lancashire, known for producing high-quality pharmaceutical products for both UK and international markets.
Are you a skilled QC Analyst with a passion for pharmaceutical quality and compliance? Do you thrive in a GMP-regulated environment and enjoy working with cutting-edge analytical techniques? If so, we want to hear from you!
QC Analyst
Lancashire - commutable from Southport, Wigan, Preston, Blackburn, Clitheroe, Bury, Darwen.
Up to £35,000 per annum
As a QC Analyst, you will play a key role in ensuring the safety, efficacy, and compliance of pharmaceutical products through rigorous analytical testing.
The responsibilities of the QC Analyst include:
• Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.
• Operate and maintain analytical instruments including HPLC, GC, UV, and IR.
• Perform equipment calibration and ensure accurate documentation.
• Investigate and document Out of Specification (OOS) and Out of Trend (OOT) results.
• Support method development and validation activities.
• Ensure strict adherence to cGMP and internal quality standards.
• Compile, interpret, and report analytical data for R&D and regulatory purposes.
The ideal candidate for the QC Analyst post will have:
• BSc (or higher) in Chemistry, Pharmaceutical Sciences, or a related discipline.
• 1–3 years of experience in a GMP-regulated pharmaceutical laboratory.
• Proficient in HPLC; experience with GC, UV, and IR is advantageous.
• Strong attention to detail and ability to work independently.
• Familiarity with regulatory guidelines (MHRA, FDA, ICH) is a plus.
In return, you’ll join a supportive team with opportunities for professional development, ongoing training, and career progression within a growing pharmaceutical business.